JP2005511543A5 - - Google Patents
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- JP2005511543A5 JP2005511543A5 JP2003537644A JP2003537644A JP2005511543A5 JP 2005511543 A5 JP2005511543 A5 JP 2005511543A5 JP 2003537644 A JP2003537644 A JP 2003537644A JP 2003537644 A JP2003537644 A JP 2003537644A JP 2005511543 A5 JP2005511543 A5 JP 2005511543A5
- Authority
- JP
- Japan
- Prior art keywords
- oxo
- methyl
- hydroxy
- alkyl
- carboxamide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 125000000217 alkyl group Chemical group 0.000 claims 123
- 125000001424 substituent group Chemical group 0.000 claims 76
- -1 -OH Chemical group 0.000 claims 33
- 229910052736 halogen Inorganic materials 0.000 claims 33
- 150000002367 halogens Chemical group 0.000 claims 32
- 125000005842 heteroatoms Chemical group 0.000 claims 29
- 229910052760 oxygen Inorganic materials 0.000 claims 28
- 229910052717 sulfur Inorganic materials 0.000 claims 28
- 125000003118 aryl group Chemical group 0.000 claims 27
- 125000000623 heterocyclic group Chemical group 0.000 claims 25
- 125000001072 heteroaryl group Chemical group 0.000 claims 19
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 19
- 150000001875 compounds Chemical class 0.000 claims 18
- 125000004043 oxo group Chemical group O=* 0.000 claims 16
- 150000003839 salts Chemical class 0.000 claims 12
- 239000011780 sodium chloride Substances 0.000 claims 12
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 11
- 125000004176 4-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1F)C([H])([H])* 0.000 claims 10
- 150000003857 carboxamides Chemical class 0.000 claims 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 6
- 125000002877 alkyl aryl group Chemical group 0.000 claims 5
- 125000002619 bicyclic group Chemical group 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 4
- 125000004485 2-pyrrolidinyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])C1([H])* 0.000 claims 4
- 125000004432 carbon atoms Chemical group C* 0.000 claims 4
- 125000001188 haloalkyl group Chemical group 0.000 claims 4
- MMPZNODECHHWIW-UHFFFAOYSA-N N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-2-(4-methylmorpholin-3-yl)-6-oxopyrimidine-4-carboxamide Chemical compound CN1CCOCC1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C MMPZNODECHHWIW-UHFFFAOYSA-N 0.000 claims 3
- 125000002837 carbocyclic group Chemical group 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 125000002950 monocyclic group Chemical group 0.000 claims 3
- 125000001624 naphthyl group Chemical group 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000006705 (C5-C7) cycloalkyl group Chemical group 0.000 claims 2
- CZFFBEXEKNGXKS-UHFFFAOYSA-N Raltegravir Chemical compound O1C(C)=NN=C1C(=O)NC(C)(C)C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C CZFFBEXEKNGXKS-UHFFFAOYSA-N 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 125000003709 fluoroalkyl group Chemical group 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 2
- 230000002265 prevention Effects 0.000 claims 2
- HKSQZEGSMBFHGC-UHFFFAOYSA-N pyrimidine-4-carboxamide Chemical compound NC(=O)C1=CC=NC=N1 HKSQZEGSMBFHGC-UHFFFAOYSA-N 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 1
- HALJILNZFAWGDL-UHFFFAOYSA-N 1-[2-(dimethylamino)ethyl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-2-(2-methylphenyl)-6-oxopyrimidine-4-carboxamide Chemical compound OC=1C(=O)N(CCN(C)C)C(C=2C(=CC=CC=2)C)=NC=1C(=O)NCC1=CC=C(F)C=C1 HALJILNZFAWGDL-UHFFFAOYSA-N 0.000 claims 1
- INUPCGQJKUVPAZ-UHFFFAOYSA-N 1-[2-(dimethylamino)ethyl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-6-oxopyrimidine-4-carboxamide Chemical compound O=C1N(CCN(C)C)C=NC(C(=O)NCC=2C=CC(F)=CC=2)=C1O INUPCGQJKUVPAZ-UHFFFAOYSA-N 0.000 claims 1
- HBODMPJFESBLQE-UHFFFAOYSA-N 1-[[3-[(dimethylamino)methyl]phenyl]methyl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-6-oxopyrimidine-4-carboxamide Chemical compound CN(C)CC1=CC=CC(CN2C(C(O)=C(C(=O)NCC=3C=CC(F)=CC=3)N=C2)=O)=C1 HBODMPJFESBLQE-UHFFFAOYSA-N 0.000 claims 1
- ZUEYJJHLMMKJSS-UHFFFAOYSA-N 2-(1,2-dimethyl-4-methylsulfonylpiperazin-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CN1CCN(S(C)(=O)=O)CC1(C)C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C ZUEYJJHLMMKJSS-UHFFFAOYSA-N 0.000 claims 1
- HTUOQGFZWIWCSK-UHFFFAOYSA-N 2-(1,4-dimethylpiperazin-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound C1N(C)CCN(C)C1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C HTUOQGFZWIWCSK-UHFFFAOYSA-N 0.000 claims 1
- ZWZSSLLTACAMTK-UHFFFAOYSA-N 2-(1-acetylpyrrolidin-2-yl)-5-hydroxy-1-methyl-N-[(2-methylsulfanylphenyl)methyl]-6-oxopyrimidine-4-carboxamide Chemical compound CSC1=CC=CC=C1CNC(=O)C1=C(O)C(=O)N(C)C(C2N(CCC2)C(C)=O)=N1 ZWZSSLLTACAMTK-UHFFFAOYSA-N 0.000 claims 1
- NMUQSBDHGNXUKW-UHFFFAOYSA-N 2-(1-acetylpyrrolidin-2-yl)-5-hydroxy-N-[(2-methoxyphenyl)methyl]-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound COC1=CC=CC=C1CNC(=O)C1=C(O)C(=O)N(C)C(C2N(CCC2)C(C)=O)=N1 NMUQSBDHGNXUKW-UHFFFAOYSA-N 0.000 claims 1
- UNWSVMJDBKFGES-UHFFFAOYSA-N 2-(1-acetylpyrrolidin-2-yl)-N-[(2,3-dimethoxyphenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound COC1=CC=CC(CNC(=O)C2=C(C(=O)N(C)C(C3N(CCC3)C(C)=O)=N2)O)=C1OC UNWSVMJDBKFGES-UHFFFAOYSA-N 0.000 claims 1
- AIIQXBVWKSDGKV-UHFFFAOYSA-N 2-(1-acetylpyrrolidin-2-yl)-N-[(2-ethoxyphenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CCOC1=CC=CC=C1CNC(=O)C1=C(O)C(=O)N(C)C(C2N(CCC2)C(C)=O)=N1 AIIQXBVWKSDGKV-UHFFFAOYSA-N 0.000 claims 1
- BWOYEQBLDGFHHV-UHFFFAOYSA-N 2-(1-acetylpyrrolidin-2-yl)-N-[(4-fluoro-2-methylsulfonylphenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CC(=O)N1CCCC1C1=NC(C(=O)NCC=2C(=CC(F)=CC=2)S(C)(=O)=O)=C(O)C(=O)N1C BWOYEQBLDGFHHV-UHFFFAOYSA-N 0.000 claims 1
- SXBRRPCHWCRBGM-UHFFFAOYSA-N 2-(1-acetylpyrrolidin-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CC(=O)N1CCCC1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C SXBRRPCHWCRBGM-UHFFFAOYSA-N 0.000 claims 1
- FHAGWXHXFUVYQQ-UHFFFAOYSA-N 2-(1-acetylpyrrolidin-2-yl)-N-[[2-(dimethylamino)phenyl]methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CN(C)C1=CC=CC=C1CNC(=O)C1=C(O)C(=O)N(C)C(C2N(CCC2)C(C)=O)=N1 FHAGWXHXFUVYQQ-UHFFFAOYSA-N 0.000 claims 1
- GVTUUPQFRYGXMA-UHFFFAOYSA-N 2-(1-benzoyl-2,3-dihydroindol-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound OC=1C(=O)N(C)C(C2N(C3=CC=CC=C3C2)C(=O)C=2C=CC=CC=2)=NC=1C(=O)NCC1=CC=C(F)C=C1 GVTUUPQFRYGXMA-UHFFFAOYSA-N 0.000 claims 1
- OIDDKWLJNSSGGV-UHFFFAOYSA-N 2-(1-benzoyl-4-methylpiperazin-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound C1N(C)CCN(C(=O)C=2C=CC=CC=2)C1C(N(C(=O)C=1O)C)=NC=1C(=O)NCC1=CC=C(F)C=C1 OIDDKWLJNSSGGV-UHFFFAOYSA-N 0.000 claims 1
- UYIXIEHDYTWNJZ-UHFFFAOYSA-N 2-(1-benzoylpiperidin-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound OC=1C(=O)N(C)C(C2N(CCCC2)C(=O)C=2C=CC=CC=2)=NC=1C(=O)NCC1=CC=C(F)C=C1 UYIXIEHDYTWNJZ-UHFFFAOYSA-N 0.000 claims 1
- QRIHGCAEXUHLOW-UHFFFAOYSA-N 2-(1-benzoylpyrrolidin-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound OC=1C(=O)N(C)C(C2N(CCC2)C(=O)C=2C=CC=CC=2)=NC=1C(=O)NCC1=CC=C(F)C=C1 QRIHGCAEXUHLOW-UHFFFAOYSA-N 0.000 claims 1
- NIRJXSNAERBOTN-UHFFFAOYSA-N 2-(1-benzylpiperidin-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound OC=1C(=O)N(C)C(C2N(CCCC2)CC=2C=CC=CC=2)=NC=1C(=O)NCC1=CC=C(F)C=C1 NIRJXSNAERBOTN-UHFFFAOYSA-N 0.000 claims 1
- RPTNZNNUJDCPCA-UHFFFAOYSA-N 2-(1-benzylpiperidin-3-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound OC=1C(=O)N(C)C(C2CN(CC=3C=CC=CC=3)CCC2)=NC=1C(=O)NCC1=CC=C(F)C=C1 RPTNZNNUJDCPCA-UHFFFAOYSA-N 0.000 claims 1
- RNIPBSWCXDEYGJ-UHFFFAOYSA-N 2-(1-ethyl-2,3-dihydroindol-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound C1C2=CC=CC=C2N(CC)C1C(N(C(=O)C=1O)C)=NC=1C(=O)NCC1=CC=C(F)C=C1 RNIPBSWCXDEYGJ-UHFFFAOYSA-N 0.000 claims 1
- DSYZHJDLBCRDPT-UHFFFAOYSA-N 2-(2,2-dimethoxyethyl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound O=C1N(C)C(CC(OC)OC)=NC(C(=O)NCC=2C=CC(F)=CC=2)=C1O DSYZHJDLBCRDPT-UHFFFAOYSA-N 0.000 claims 1
- RSNBQZPGNYQALO-UHFFFAOYSA-N 2-(2,3-dihydro-1H-indol-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound OC=1C(=O)N(C)C(C2NC3=CC=CC=C3C2)=NC=1C(=O)NCC1=CC=C(F)C=C1 RSNBQZPGNYQALO-UHFFFAOYSA-N 0.000 claims 1
- FGCQVGQJXOFNDP-UHFFFAOYSA-N 2-(2-acetamidopropan-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound O=C1N(C)C(C(C)(C)NC(=O)C)=NC(C(=O)NCC=2C=CC(F)=CC=2)=C1O FGCQVGQJXOFNDP-UHFFFAOYSA-N 0.000 claims 1
- VENKFOMMRMCXSN-UHFFFAOYSA-N 2-(3-acetyl-1,3-thiazolidin-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CC(=O)N1CCSC1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C VENKFOMMRMCXSN-UHFFFAOYSA-N 0.000 claims 1
- NFEPQYVYHPMREC-UHFFFAOYSA-N 2-(4-acetyl-1,2-dimethylpiperazin-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CN1CCN(C(C)=O)CC1(C)C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C NFEPQYVYHPMREC-UHFFFAOYSA-N 0.000 claims 1
- DYGQWEZNJAWTMH-UHFFFAOYSA-N 2-(4-acetyl-1-methylpiperazin-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CN1CCN(C(C)=O)CC1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C DYGQWEZNJAWTMH-UHFFFAOYSA-N 0.000 claims 1
- BMTUWFRODUAELZ-UHFFFAOYSA-N 2-(4-benzoyl-1-methylpiperazin-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CN1CCN(C(=O)C=2C=CC=CC=2)CC1C(N(C(=O)C=1O)C)=NC=1C(=O)NCC1=CC=C(F)C=C1 BMTUWFRODUAELZ-UHFFFAOYSA-N 0.000 claims 1
- KICKGPQKASOONE-UHFFFAOYSA-N 2-(4-ethyl-1-methylpiperazin-2-yl)-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound C1N(CC)CCN(C)C1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C KICKGPQKASOONE-UHFFFAOYSA-N 0.000 claims 1
- DWVBVURKCZQKOS-HUUCEWRRSA-N 2-[(2R,4R)-1-[2-(dimethylamino)-2-oxoacetyl]-4-methoxypyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CN(C)C(=O)C(=O)N1C[C@H](OC)C[C@@H]1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C DWVBVURKCZQKOS-HUUCEWRRSA-N 0.000 claims 1
- VWXCOJBXZNKXDR-HZPDHXFCSA-N 2-[(2R,4R)-1-acetyl-4-ethoxypyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CC(=O)N1C[C@H](OCC)C[C@@H]1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C VWXCOJBXZNKXDR-HZPDHXFCSA-N 0.000 claims 1
- WKDOSXUSFIHGPZ-HUUCEWRRSA-N 2-[(2R,4R)-1-acetyl-4-methoxypyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CC(=O)N1C[C@H](OC)C[C@@H]1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C WKDOSXUSFIHGPZ-HUUCEWRRSA-N 0.000 claims 1
- KQGKCKYQHCMVBU-RTBURBONSA-N 2-[(2R,4R)-1-benzoyl-4-methoxypyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound N1([C@H](C[C@H](C1)OC)C=1N(C(=O)C(O)=C(C(=O)NCC=2C=CC(F)=CC=2)N=1)C)C(=O)C1=CC=CC=C1 KQGKCKYQHCMVBU-RTBURBONSA-N 0.000 claims 1
- GUPLVGUUZBBMSC-HUUCEWRRSA-N 2-[(2R,4R)-4-ethoxy-1-[2-(methylamino)-2-oxoacetyl]pyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CNC(=O)C(=O)N1C[C@H](OCC)C[C@@H]1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C GUPLVGUUZBBMSC-HUUCEWRRSA-N 0.000 claims 1
- ALTIACWYHGENDH-ZDUSSCGKSA-N 2-[(2S)-1-[2-(dimethylamino)-2-oxoacetyl]-4,4-difluoropyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CN(C)C(=O)C(=O)N1CC(F)(F)C[C@H]1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C ALTIACWYHGENDH-ZDUSSCGKSA-N 0.000 claims 1
- IZAMFVNHGWAIIH-AWEZNQCLSA-N 2-[(2S)-1-[2-(dimethylamino)-2-oxoacetyl]pyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CN(C)C(=O)C(=O)N1CCC[C@H]1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C IZAMFVNHGWAIIH-AWEZNQCLSA-N 0.000 claims 1
- JJMZDFZRSSKHCW-ZDUSSCGKSA-N 2-[(2S)-1-acetyl-4,4-difluoropyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CC(=O)N1CC(F)(F)C[C@H]1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C JJMZDFZRSSKHCW-ZDUSSCGKSA-N 0.000 claims 1
- SXBRRPCHWCRBGM-AWEZNQCLSA-N 2-[(2S)-1-acetylpyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CC(=O)N1CCC[C@H]1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C SXBRRPCHWCRBGM-AWEZNQCLSA-N 0.000 claims 1
- VBNMBVHOVXGRIT-HNNXBMFYSA-N 2-[(2S)-4,4-difluoro-1-(pyrazine-2-carbonyl)pyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound OC=1C(=O)N(C)C([C@H]2N(CC(F)(F)C2)C(=O)C=2N=CC=NC=2)=NC=1C(=O)NCC1=CC=C(F)C=C1 VBNMBVHOVXGRIT-HNNXBMFYSA-N 0.000 claims 1
- OLQXVJVOJZSEHE-HNNXBMFYSA-N 2-[(2S)-4,4-difluoro-1-(pyridazine-3-carbonyl)pyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound OC=1C(=O)N(C)C([C@H]2N(CC(F)(F)C2)C(=O)C=2N=NC=CC=2)=NC=1C(=O)NCC1=CC=C(F)C=C1 OLQXVJVOJZSEHE-HNNXBMFYSA-N 0.000 claims 1
- VXMCFIODWHQIEV-INIZCTEOSA-N 2-[(2S)-4,4-difluoro-1-(pyridine-2-carbonyl)pyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound OC=1C(=O)N(C)C([C@H]2N(CC(F)(F)C2)C(=O)C=2N=CC=CC=2)=NC=1C(=O)NCC1=CC=C(F)C=C1 VXMCFIODWHQIEV-INIZCTEOSA-N 0.000 claims 1
- RSZZZMBAKCZCMS-LBPRGKRZSA-N 2-[(2S)-4,4-difluoro-1-methylpyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CN1CC(F)(F)C[C@H]1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C RSZZZMBAKCZCMS-LBPRGKRZSA-N 0.000 claims 1
- WGVOGOWLJMYYJM-KGLIPLIRSA-N 2-[(2S,4R)-1-acetyl-4-hydroxypyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound CC(=O)N1C[C@H](O)C[C@H]1C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C WGVOGOWLJMYYJM-KGLIPLIRSA-N 0.000 claims 1
- FOSNNBJCOZOKQS-RTWAWAEBSA-N 2-[(2S,4R)-1-acetyl-4-phenylmethoxypyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound OC=1C(=O)N(C)C([C@@H]2C[C@H](CN2C(=O)C)OCC=2C=CC=CC=2)=NC=1C(=O)NCC1=CC=C(F)C=C1 FOSNNBJCOZOKQS-RTWAWAEBSA-N 0.000 claims 1
- XWCKLKLAVPVPPD-MSOLQXFVSA-N 2-[(2S,4R)-1-benzoyl-4-hydroxypyrrolidin-2-yl]-N-[(4-fluorophenyl)methyl]-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxamide Chemical compound OC=1C(=O)N(C)C([C@H]2N(C[C@H](O)C2)C(=O)C=2C=CC=CC=2)=NC=1C(=O)NCC1=CC=C(F)C=C1 XWCKLKLAVPVPPD-MSOLQXFVSA-N 0.000 claims 1
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- 125000004574 piperidin-2-yl group Chemical group N1C(CCCC1)* 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 claims 1
- 0 *C(N(*)C1=O)=NC(C(N(*)*)=O)=C1O Chemical compound *C(N(*)C1=O)=NC(C(N(*)*)=O)=C1O 0.000 description 1
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| US6642245B1 (en) | 1990-02-01 | 2003-11-04 | Emory University | Antiviral activity and resolution of 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane |
| US5637618A (en) | 1990-06-01 | 1997-06-10 | Bioresearch, Inc. | Specific eatable taste modifiers |
| DE4029654A1 (de) | 1990-09-19 | 1992-04-02 | Hoechst Ag | 2-phenyl-pyrimidine, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung als fungizide |
| US5519021A (en) | 1992-08-07 | 1996-05-21 | Merck & Co., Inc. | Benzoxazinones as inhibitors of HIV reverse transcriptase |
| TW287160B (ru) | 1992-12-10 | 1996-10-01 | Hoffmann La Roche | |
| US5919776A (en) * | 1996-12-20 | 1999-07-06 | Merck & Co., Inc. | Substituted aminoquinolines as modulators of chemokine receptor activity |
| US5935946A (en) | 1997-07-25 | 1999-08-10 | Gilead Sciences, Inc. | Nucleotide analog composition and synthesis method |
| US6632823B1 (en) | 1997-12-22 | 2003-10-14 | Merck & Co., Inc. | Substituted pyridine compounds useful as modulators of acetylcholine receptors |
| JP3794469B2 (ja) | 1998-03-26 | 2006-07-05 | 塩野義製薬株式会社 | 抗ウイルス作用を有するインドール誘導体 |
| US6306891B1 (en) | 1998-06-03 | 2001-10-23 | Merck & Co., Inc. | HIV integrase inhibitors |
| WO1999062520A1 (en) | 1998-06-03 | 1999-12-09 | Merck & Co., Inc. | Hiv integrase inhibitors |
| EP1086091A4 (en) | 1998-06-03 | 2001-10-10 | Merck & Co Inc | HIV INTEGRASE INHIBITORS |
| DE69937405T2 (de) | 1998-08-20 | 2008-02-14 | Toyama Chemical Co. Ltd. | Stickstoffheterocyclische Carboxamidverbindungen oder deren Salze als antivirale Mittel |
| AP2001002169A0 (en) | 1998-12-25 | 2001-06-30 | Shionogi & Co | Aromatic heterocycle compounds having hiv intergrase inhibiting activities |
| JP2002538144A (ja) * | 1999-03-04 | 2002-11-12 | コリア・リサーチ・インスティテュート・オブ・ケミカル・テクノロジー | 抗ウイルス性２，４−ピリミジンジオン誘導体およびその製造方法 |
| JP2003503386A (ja) | 1999-06-25 | 2003-01-28 | メルク エンド カムパニー インコーポレーテッド | １−（芳香族またはヘテロ芳香族置換）−３−（ヘテロ芳香族置換）−１，３−プロパンジオン類およびそれの使用 |
| EP1282606B1 (en) * | 2000-05-08 | 2015-04-22 | Janssen Pharmaceutica NV | Hiv replication inhibiting pyrimidines and triazines |
| GB0017676D0 (en) | 2000-07-19 | 2000-09-06 | Angeletti P Ist Richerche Bio | Inhibitors of viral polymerase |
| US20050010048A1 (en) | 2000-10-12 | 2005-01-13 | Linghang Zhuang | Aza-and polyaza-naphthalenly ketones useful as hiv integrase inhibitors |
| IL155089A0 (en) | 2000-10-12 | 2003-10-31 | Merck & Co Inc | Aza and polyaza-naphthalenyl carboxamides useful as hiv integrase inhibitors |
| ATE364385T1 (de) | 2000-10-12 | 2007-07-15 | Merck & Co Inc | Aza- und polyaza-naphthalenylcarbonsäureamide als hiv-integrase-hemmer |
| EP1326610B1 (en) | 2000-10-12 | 2006-11-15 | Merck & Co., Inc. | Aza-and polyaza-naphthalenyl carboxamides useful as hiv integrase inhibitors |
| MXPA03007765A (es) | 2001-03-01 | 2003-12-08 | Shionogi & Co | Compuestos heteroarilo que contienen nitrogeno, que tienen actividad inhibitoria contra virus de inmunodeficiencia humana integrasa. |
| ATE530520T1 (de) | 2001-08-10 | 2011-11-15 | Shionogi & Co | Antivirales mittel |
| EA007060B1 (ru) * | 2001-10-26 | 2006-06-30 | Иституто Ди Ричерке Ди Биолоджиа Молеколаре П. Анджелетти Спа | N-замещённые гидроксипиримидинон-карбоксамидные ингибиторы вич интегразы |
| DE60218511T2 (de) | 2001-10-26 | 2007-10-25 | Istituto Di Richerche Di Biologia Molecolare P. Angeletti S.P.A. | Dihydroxypyrimidin-carbonsäueramid-hemmer der hiv-integrase |
| WO2003047564A1 (fr) | 2001-12-05 | 2003-06-12 | Shionogi & Co., Ltd. | Dérivé ayant une activité d'inhibition de l'intégrase du vih |
| AU2003248872A1 (en) | 2002-07-09 | 2004-01-23 | Bristol-Myers Squibb Company | Hiv integrase inhibitors |
| SK2662004A3 (sk) | 2002-11-20 | 2005-06-02 | Japan Tobacco, Inc. | Zlúčenina s obsahom 4-oxochinolínu a jej použitie ako inhibítora integráz |
| WO2004062613A2 (en) | 2003-01-13 | 2004-07-29 | Bristol-Myers Squibb Company | Hiv integrase inhibitors |
| US7037908B2 (en) | 2003-04-24 | 2006-05-02 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
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2002
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- 2002-10-21 DK DK02801950T patent/DK1441735T3/da active
- 2002-10-21 SI SI200230296T patent/SI1441735T1/sl unknown
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- 2002-10-21 WO PCT/GB2002/004753 patent/WO2003035077A1/en active IP Right Grant
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- 2004-04-26 HR HRP20040373AA patent/HRP20040373B1/xx not_active IP Right Cessation
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- 2008-04-11 CY CY200800008C patent/CY2008008I1/el unknown
- 2008-04-18 LT LTPA2008007C patent/LTC1441735I2/lt unknown
- 2008-06-06 NO NO2008007C patent/NO2008007I1/no not_active IP Right Cessation
- 2008-06-17 FR FR08C0026C patent/FR08C0026I2/fr active Active
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- 2010-09-17 US US12/884,734 patent/US20110034449A1/en not_active Abandoned
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